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NCT01801202 · ClinicalTrials.gov registry record · NA
Clinical Evaluation of LightSheer Duet 805nm HS Handpiece
A NA study, sponsored by Lumenis Be.
- Completed
- Registry status
- NA
- Development phase
- 21
- Enrollment target
NCT01801202: Completed NA study, sponsored by Lumenis Be.
NCT01801202 is a NA study that has completed, run by Lumenis Be. The registered enrollment target is 21 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01801202, a NA study, has completed, sponsored by Lumenis Be.
- COMPLETED
- Registry status
- NA
- Development phase
- 21 participants
- Enrollment target
Study Summary
* The study will re-confirm that the LightSheer Duet HS 805 nm handpiece is safe for removal of unwanted hair, and will result in hair removal and permanent hair count reduction. * Twenty (20)subjects, Fitzpatrick Skin Type I-IV will be included in a single site. * Each subject will receive five treatments at four to six week intervals and return for follow-up visits at three and six months after the last treatment for evaluation of the treated areas.
Primary Outcome
To evaluate the safety of hair removal using the LightSheer Duet HS 805 nm handpiece
Interventions
- DEVICE LightSheer Duet HS handpiece
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 21 participants |
| Start Date | 2013-02 |
| Est. Completion | 2014-11 |
| Phase | NA |
What the finished NCT01801202 record still lists
NCT01801202 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which LightSheer Duet HS handpiece is the first listed.
NCT01801202 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01801202 about?
NCT01801202 is a clinical study titled "Clinical Evaluation of LightSheer Duet 805nm HS Handpiece". * The study will re-confirm that the LightSheer Duet HS 805 nm handpiece is safe for removal of unwanted hair, and will result in hair removal and permanent hair count reduction. * Twenty (20)subjects, Fitzpatrick Skin Type I-IV will be included in a single site. * Each subject will receive five tre...
What is the current status of trial NCT01801202?
This trial is currently completed. It is a NA study. The enrollment target is 21 participants. The study started on 2013-02. Estimated completion is 2014-11.
What interventions are being tested in trial NCT01801202?
The interventions under investigation include: LightSheer Duet HS handpiece (DEVICE).
Who is sponsoring clinical trial NCT01801202?
This trial is sponsored by Lumenis Be, which has 20 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01801202's enrollment target sits among peer trials
21 1762nd of 2000 higher than 233 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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